The story of Dylan
~Hi, my name is Wanda McCune, & my son Dylan Sharp, who was diagnosed in November of 2015 with a Rare Neurological Movement Disorder at age 10.
~We knew in February of 2015 that Dylan had some type of movement disorder, but we had to wait for a long series of test results to come back before we knew what type of movement disorder that Dylan had, & that it was Rare. The only thing that we know about it is that he has Calcifications on his brain & basal (brain), & that it falls under a movement disorder. This is a battle that Dylan faces daily. To learn more about Dylan’s Rare disease, & movement disorders in children visit our website @ http://www.welcometodylansjourney.com. You can also, read our Blog, then connect with Dylan @ Facebook.com/WelcometoDylansJourney called: Join the Movement & Pray for Dylan. To help us battle this rare disease, support Dylan with spirit, & the power of prayer, all while also helping us bring awareness to this horrible disease. Thank You All.